8IY5
ETB-Gi complex bound to endothelin-1
8IY5 の概要
| エントリーDOI | 10.2210/pdb8iy5/pdb |
| EMDBエントリー | 35814 |
| 分子名称 | Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (6 entities in total) |
| 機能のキーワード | class a gpcr, endothelin, gi, vasoactive peptide, peptide binding protein |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 186159.85 |
| 構造登録者 | |
| 主引用文献 | Sano, F.K.,Akasaka, H.,Shihoya, W.,Nureki, O. Cryo-EM structure of the endothelin-1-ET B -G i complex. Elife, 12:-, 2023 Cited by PubMed Abstract: The endothelin ET receptor is a promiscuous G-protein coupled receptor that is activated by vasoactive peptide endothelins. ET signaling induces reactive astrocytes in the brain and vasorelaxation in vascular smooth muscle. Consequently, ET agonists are expected to be drugs for neuroprotection and improved anti-tumor drug delivery. Here, we report the cryo-electron microscopy structure of the endothelin-1-ET-G complex at 2.8 Å resolution, with complex assembly stabilized by a newly established method. Comparisons with the inactive ET receptor structures revealed how endothelin-1 activates the ET receptor. The NPxxY motif, essential for G-protein activation, is not conserved in ET, resulting in a unique structural change upon G-protein activation. Compared with other GPCR-G-protein complexes, ET binds G in the shallowest position, further expanding the diversity of G-protein binding modes. This structural information will facilitate the elucidation of G-protein activation and the rational design of ET agonists. PubMed: 37096326DOI: 10.7554/eLife.85821 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.8 Å) |
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